Detection and typing of bacterial strains

ABSTRACT

Methods for the detection and typing of bacterial strains from food products and dietary supplements, environmental samples, in vivo/in vitro samples, and for studying the natural diversity of the species are disclosed. Potential applications also include product development and/or detection and differentiation of new bacterial strains.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application Ser. No. 60/566,007, filed Apr. 28, 2004, the contents of which are hereby incorporated in their entirety by reference herein.

FIELD OF THE INVENTION

This invention relates to methods for detecting and typing bacterial strains, specifically Lactobacillus strains.

BACKGROUND OF THE INVENTION

Rapid and accurate differentiation of bacterial strains is important when making medical diagnoses, in epidemiological studies, and for studying evolutionary diversity among bacteria. Various methods exist for typing or detecting bacterial strains, including RFLP, hybridization, and sequencing. Epidemiologically informative microsatellite DNA polymorphisms have been observed in different strains of Helicobacter pylori (Marshall et al. (1996) J. Appl. Bacteria 81:509-517). Similarly, repetitive DNA elements of Mycobacterium tuberculosis have been used for efficient strain tracking (Van Soolingen et al. (1993) J. Clin. Microbiol. 31:1987-1995). In addition, short sequence repeat (SSR) variation has been used to differentiate the strains of Haemophilus influenzae isolated from different patients (van Belkum et al. (1997) Infect. Immun. 65:5017-5027). However, current methods available to specifically differentiate bacterial strains, such as Lactobacillus acidophilus strains, are based either on 16SrRNA gene sequencing, which is only accurate to the species level, or on long and difficult Pulsed Field Gel Electrophoresis (PFGE) procedures.

The CRISPR (Clustered Regularly Interspaced Short Palindromic Repeat; also called SPIDR (Spacers Interspersed Direct Repeats), VNTR (Variable Number of Tandem Repeats), SRVR (Short Regularly Variable Repeats), and SRSR (Short Regularly Spaced Repeats)) loci, described by Jansen et al. (2002) OMICS J. Integr. Biol. 6:23-33, constitute a novel family of repeat sequences that is present in Bacteria and Archaea but not in Eukarya. The repeat loci typically consist of repetitive stretches of nucleotides with a length of 25 to 37 base pairs alternated by nonrepetitive DNA spacers of approximately equal length. To date, CRISPR loci have been identified in more than forty microorganisms (Jansen et aL (2002) OMICS J. Integr. Biol. 6:23-33), but from the lactic acid bacteria, they have only been described from Streptococcus species. Despite their discovery over 15 years ago in E. coli (Ishino et al. (1987) J. Bacteriol. 169:5429-5433), no physiological function has yet been discovered. The nucleotide sequences of the repeats are generally highly conserved within a species, but show low similarity between species. It has also been shown that variability among CRISPR loci is not due primarily to single nucleotide base changes, but rather to deletions/insertions of entire repeat and spacer regions. These properties have led to the use of the CRISPR loci as a strain-typing tool in Mycobacterium (Groenen et al. (1993) Mol. Microbiol. 10:1057-1065).

As methods to differentiate Lactobacillus bacteria, specifically L. acidophilus, are either not accurate to the strain level or are technically demanding, the development of new methods for differentiating Lactobacillus strains is desirable.

BRIEF SUMMARY OF THE INVENTION

Compositions and methods for detecting and typing bacteria are provided, particularly a Lactobacillus strain of bacteria, for example a Lactobacillus acidophilus strain. Compositions of the invention include isolated nucleic acid molecules from Lactobacillus acidophilus comprising a region of DNA, preferably located between the genes for DNA polymerase I (polA) and a putative phosphoribosylamine-glycine ligase (purD), consisting of one or more copies of a repetitive DNA sequence of about 20-40 base pairs, such as about 25-35 base pairs or of about 27-30 base pairs, interspersed with nonrepetitive spacer sequences of about the same length. In one embodiment, the isolated nucleic acid molecule comprises a 29 base pair sequence that is present 32 times, and is separated by the same number of 32-base pair spacer sequences.

Compositions of the invention also include isolated nucleic acid molecules from Lactobacillus brevis, Lactobacillus casei, and Lactobacillus delbrueckii ssp. bulgaricus comprising repetitive sequences originally identified in a CRISPR region. In one embodiment, the isolated nucleic acid molecule comprises a 28 base pair sequence from L. brevis. In another embodiment, the isolated nucleic acid molecule comprises a 28 base pair sequence from L. casei. In yet another embodiment, the isolated nucleic acid molecule comprises a 28 base pair sequence from L. delbrueckii ssp. bulgaricus.

Variant nucleic acid molecules sufficiently identical to the nucleotide sequences are also encompassed by the present invention. Additionally, fragments and sufficiently identical fragments of the nucleotide sequences are encompassed. Specifically, the present invention provides for isolated nucleic acid molecules comprising one or more nucleotide sequences found in SEQ ID NOS:1-50. The present invention further provides for isolated nucleic acid molecules comprising 1-140 repeats of a nucleotide sequence of the invention, or a variant thereof. In some embodiments, the isolated nucleic acid molecules comprise more than 5 repeats, more than 10 repeats, less than 50 repeats, or less than 35 repeats of a nucleotide sequence of the invention, or a variant thereof. Compositions also include PCR primers for amplifying this region in a Lactobacillus species, including L. acidophilus, L. brevis, L. casei and L. delbrueckii. Nucleotide sequences that are complementary to a nucleotide sequence of the invention, or that hybridize to a sequence of the invention, are also encompassed. Further are included methods and kits for detecting the presence of a nucleic acid sequence of the invention in a sample, and methods and kits for typing bacteria, including Lactobacillus strains, particularly L. acidophilus, L. brevis, L. casei and L. delbrueckii strains.

Methods for typing a bacterium having a CRISPR region are provided. The methods comprise obtaining a sample comprising the bacterium; amplifying a region of DNA comprising the CRISPR region or a fragment thereof in the sample to create amplified DNA; adding to the amplified DNA at least one restriction enzyme that recognizes one or more sites in the amplified DNA; incubating the restriction enzyme with the amplified DNA for a time sufficient to form restriction fragments; determining the number of the restriction fragments and their size; and typing the bacterium based on the number and size of the restriction fragments.

A method for typing a Lactobacillus bacterial strain is also provided. The method comprises obtaining a sample, amplifying a region of DNA comprising at least one of the nucleotide sequences set forth in SEQ ID NOS:1-7 and 37-48, or a variant thereof, in the sample to create amplified DNA, and typing the bacterial strain based on the amplified DNA. The methods may further comprise adding to the amplified DNA at least one restriction enzyme that recognizes one or more sites in the amplified DNA, incubating the restriction enzyme with the amplified DNA for a time sufficient to form restriction fragments, determining the number of the restriction fragments and their size, and typing the bacterial strain based on the number and size of the restriction fragments. Alternatively, the methods may further comprise sequencing the amplified DNA to obtain sequencing results, and typing the bacterial strain based on the sequencing results. In one embodiment, the Lactobacillus is L. acidophilus.

The amplified DNA may be obtained by providing a first primer that binds to a repetitive sequence in a CRISPR region, providing a second primer that binds to DNA flanking (i.e., upstream or downstream of) the CRISPR region, using the primers in a PCR reaction to create amplified DNA, separating the amplified DNA on a gel to produce a distinct band pattern showing the number and sizes of the amplified DNA, and typing the bacterial strain based on the band pattern. The number and sizes of the bands are characteristic of the strain. The amplified DNA may alternatively be obtained by providing a first primer that binds to a region of DNA upstream of the CRISPR region, and a second primer that binds to a region of DNA downstream of the CRISPR region, using the primers in a PCR reaction to create amplified DNA, separating the amplified DNA on a gel to produce a band showing the size of the amplified CRISPR DNA, and typing the bacterial strain based on the band size. The size of the amplified DNA is characteristic of the strain.

Methods for detecting the presence of a Lactobacillus species in a sample are provided. The methods comprise obtaining a sample, amplifying a region of DNA comprising at least one of the nucleotide sequences set forth in SEQ ID NOS:1-7 and 37-48, or a variant thereof, to create amplified DNA, and detecting the amplified DNA. The methods may further comprise adding to the amplified DNA at least one restriction enzyme that recognizes one or more sites in the amplified DNA, incubating the restriction enzyme with the amplified DNA for a time sufficient to form restriction fragments, determining the number of the restriction fragments and their size, and detecting the presence of a Lactobacillus species based on the number and size of the restriction fragments. Alternatively, the methods may further comprise sequencing the amplified DNA to obtain sequencing results, and detecting the presence of a Lactobacillus species based on the sequencing results.

The methods of the present invention are useful for the detection and typing of bacterial strains, including Lactobacillus strains such as L. acidophilus, L. brevis, L. casei, and L. delbrueckii strains, in food products and dietary supplements, including animal feed and animal feed supplements, in in vivo/in vitro samples, and for studying the natural diversity of the species from environmental samples. The methods are also useful for product development and identification of new bacterial strains, particularly Lactobacillus strains.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an intergenic region in Lactobacillus acidophilus having features of a CRISPR locus.

FIG. 2 shows the nucleotide sequences of the repeat regions in the intergenic region (SEQ ID NO:1). The 29-bp repeats are highlighted (SEQ ID NOS:2-7). An imperfect inverted repeat is indicated by an underline on the last repeat. The spacer regions (SEQ ID NOS:8-35) and a flanking region (SEQ ID NO:36) are not highlighted. Two sequences are repeated in the spacer region; one is repeated twice (outlined and bold) (SEQ ID NO:15) and one is repeated three times (caps and bold) (SEQ ID NO:13).

FIG. 3 consists of micrographs of various agarose gel electrophoresis experiments. FIG. 3A shows PCR products and FIGS. 3B, C, and D show restriction fragment results. A. Lane M—1 Kb DNA ladder; Lane 1—NCFM®; Lane 2—Strain C; Lane 3—Strain D; Lane 4—ATCC 4356; Lane 5—Strain B; Lane 6—Strain E. B. Lane M—50 bp DNA ladder; Lane 1—NCFM®; Lane 2—Strain C; Lane 3—Strain D; Lane 4—ATCC 4356; Lane 5—ATCC 4357; Lane 6—Strain B. C. Lane M—50 bp DNA ladder; Lane 1—NCFM®; Lane 2—Strain C; Lane 3—Strain D; Lane 4—ATCC 4356; Lane 5—ATCC 4357; Lane 6—Strain B. D. Lane M—50 bp DNA ladder; Lane 1—NCFM®; Lane 2—Strain C; Lane 3—Strain D; Lane 4—ATCC 4356; Lane 5—ATCC 4357; Lane 6—Strain B.

FIG. 4 is a micrograph of PCR products of the following strains: Lane 1—L. acidophilus NCFM®; Lane 2—L. acidophilus Lac-1; Lane 3—L. acidophilus Lac-2; Lane 4—L. acidophilus Lac-3; Lane 5—L. acidophilus ATCC 4355; Lane 6—L. acidophilus ATCC 4356; Lane 7—L. acidophilus ATCC 4357; Lane 8—L. acidophilus ATCC 4796; Lane 9—L. helveticus ATCC 521; Lane 10—L. acidophilus ATCC 832; Lane 11—L. acidophilus ATCC 9224; Lane 12—L. acidophilus ATCC 11975; Lane 13—L. acidophilus ATCC 314; Lane 14—L. gasseri ATCC 43121; Lane 15—L. acidophilus Lac-4; Lane 16—L. acidophilus Lac-5; Lane 17—L. amylovorus ATCC 33198; Lane 18—L. gallinarum ATCC 33199; Lane 19—L. gasseri ATCC 33323; Lane 20—L. johnsonii ATCC 33200; Lane 21—L. crispatus Lcr-1; Lane 22—L. helveticus Lhe-1; Lane 23—control (no DNA).

FIG. 5 is a micrograph of bands resulting from PCR amplification followed by restriction digest of the following strains: Lane 1—L. acidophilus NCFM®; Lane 2—L. acidophilus Lac-1; Lane 3—L. acidophilus Lac-2; Lane 4—L. acidophilus Lac-3; Lane 5—L. acidophilus ATCC 4355; Lane 6—L. acidophilus ATCC 4356; Lane 7—L. acidophilus ATCC 4357; Lane 8—L. acidophilus ATCC 4796; Lane 9—L. acidophilus ATCC 832; Lane 10—L. acidophilus ATCC 9224; Lane 11—L. acidophilus ATCC 11975; Lane 12—L. acidophilus ATCC 314; Lane 13—L. acidophilus Lac-4; Lane 14—L. acidophilus Lac-5.

FIG. 6 is a micrograph showing pulsed field gel electrophoresis of L. acidophilus NCFM® (Lane 1); L. acidophilus Lac-1 (Lane 2); L. acidophilus Lac-3 (Lane 3); and L. acidophilus ATCC 4356 (Lane 4).

FIG. 7 shows a repeat sequence from L. acidophilus (Lac) (SEQ ID NO:37); L. brevis (Lbr) (SEQ ID NO:38); L. casei (Lca) (SEQ ID NO:45); and L. delbrueckii ssp. Bulgaricus (Lde) (SEQ ID NO:46). Variant nucleotides and their positions are shown below the main sequence.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to methods and compositions for detecting and/or typing bacterial strains, such as Lactobacillus strains, including Lactobacillus acidophilus, L. brevis, L. casei, and L. delbrueckii. These methods can be used in medical and food safety diagnostics, or in research. By “typing” or “differentiation” is intended the identification of the strain of a bacterium, including identifying that it is distinct from other strains based on its nucleotide sequence (i.e., by analyzing the band pattern resulting from restriction enzyme digestion). By “detection” is intended the verification of the presence or absence of a species of bacteria in a sample. Compositions of the invention include isolated nucleic acid molecules from L. acidophilus, L. brevis, L. casei, and L. delbrueckii that are part of a CRISPR locus. By “CRISPR region” or “CRISPR locus” is intended a repetitive stretch of nucleotide sequence, wherein the repeats are about 20 to about 40 base pairs in length, and are alternated by nonrepetitive DNA spacers of approximately equal size. The acronyms CRISPR, SPIDR, VNTR, and SRVR have each been used to describe a nucleotide sequence having interspaced repeats.

Additionally, the present invention provides methods and kits for bacterial typing that may be used to determine similarities and/or differences between bacterial strains, particularly Lactobacillus strains, including L. acidophilus, L. brevis, L. casei, and L. delbrueckii, and methods and kits for detecting the presence or absence of a Lactobacillus species in a sample. More particularly, the methods involve a rapid, semi-automated method for the detection and/or typing of strains of prokaryotic organisms, such as L. acidophilus, in which a CRISPR DNA sequence is amplified and used to differentiate between strains of Lactobacillus, or for the detection of a Lactobacillus species.

Isolated nucleic acid molecules of the present invention comprise the nucleotide sequences set forth in SEQ ID NOS:1-50, and variants and fragments thereof. The present invention also encompasses molecules that are complementary to these nucleic acid sequences, or that hybridize to these sequences.

The nucleic acid compositions encompassed by the present invention are isolated or substantially purified. By “isolated” or “substantially purified” is intended that the nucleic acid molecules, or biologically active fragments or variants, are substantially or essentially free from components normally found in association with the nucleic acid in its natural state. Such components include other cellular material, culture media from recombinant production, and various chemicals used in chemically synthesizing the nucleic acids. Preferably, an “isolated” nucleic acid of the present invention is free of nucleic acid sequences that flank the nucleic acid of interest in the genomic DNA of the organism from which the nucleic acid was derived (such as coding sequences present at the 5′ or 3′ ends). However, the molecule may include some additional bases or moieties that do not deleteriously affect the basic characteristics of the composition. For example, in various embodiments, the isolated nucleic acid contains less than 5 kb, 4 kb, 3 kb, 2 kb, 1 kb, 0.5 kb, or 0.1 kb of nucleic acid sequence normally associated with the genomic DNA in the cells from which it was derived.

The compositions and methods of the present invention can be used to detect Lactobacillus species, including L. acidophilus, L. brevis, L. casei, and L. delbrueckii, or to type bacterial strains, including very closely related L. acidophilus strains, both in the laboratory and in commercial products. This is useful for product development, as well as for research in bacterial species diversity and evolution, and in the identification of new bacterial strains, including new Lactobacillus strains.

Detection and Differentiation of Bacterial Strains

CRISPR loci are a distinct class of interspersed short sequence repeats (SSRs) that were first recognized in E. coli (Ishino et al. (1987) J. Bacteriol. 169:5429-5433; Nakata et al. (1989) J. Bacteriol. 171:3553-3556). Similar interspersed SSRs have been identified in Haloferax mediterranei, Streptococcus pyogenes, Anabaena, and Mycobacterium tuberculosis (Groenen et al. (1993) Mol. Microbiol. 10:1057-1065; Hoe et al. (1999) Emerg. Infect. Dis. 5:254-263; Masepohl et al. (1996) Biochim. Biophys. Acta 1307:26-30; Mojica et al. (1995) Mol. Microbiol. 17:85-93). The CRISPR loci differ from other SSRs by the structure of the repeats, which have been termed short regularly spaced repeats (SRSRs) (Janssen et al. (2002) OMICS J. Integ. Biol. 6:23-33; Mojica et al. (2000) Mol. Microbiol. 36:244-246). The repeats are short elements that occur in clusters, that are always regularly spaced by unique intervening sequences with a constant length (Mojica et al. (2000) Mol. Microbiol. 36:244-246). Although the repeat sequences are highly conserved between strains, the number of interspersed repeats and the sequences of the spacer regions differ from strain to strain (van Embden et al. (2000) J. Bacteriol. 182:2393-2401). Methods for identifying CRISPR regions are well known in the art (see, for example, the above references, which are incorporated by reference herein in their entirety, as well as the methods used in Example 1). The methods of the present invention are herein exemplified by experiments involving L. acidophilus; however, one of skill in the art would recognize that the methods may be used for detection and/or strain identification of any bacterium having a CRISPR region.

The number of nucleotides in a repeat is generally about 20 to about 40 base pairs, but may be about 20 to about 39 base pairs, about 20 to about 37 base pairs, about 20 to about 35 base pairs, about 20 to about 33 base pairs, about 20 to about 30 base pairs, about 21 to about 40 base pairs, about 21 to about 39 base pairs, about 21 to about 37 base pairs, about 23 to about 40 base pairs, about 23 to about 39 base pairs, about 23 to about 37 base pairs, about 25 to about 40 base pairs, about 25 to about 39 base pairs, about 25 to about 37 base pairs, about 25 to about 35 base pairs, or about 28 or 29 base pairs. The number of repeats may range from about 1 to about 140, from about 1 to about 100, from about 2 to about 100, from about 5 to about 100, from about 10 to about 100, from about 15 to about 100, from about 20 to about 100, from about 25 to about 100, from about 30 to about 100, from about 35 to about 100, from about 40 to about 100, from about 45 to about 100, from about 50 to about 100, from about 1 to about 135, from about 1 to about 130, from about 1 to about 125, from about 1 to about 120, from about 1 to about 115, from about 1 to about 110, from about 1 to about 105, from about 1 to about 100, from about 1 to about 95, from about 1 to about 90, from about 1 to about 80, from about 1 to about 70, from about 1 to about 60, from about 1 to about 50, from about 10 to about 140, from about 10 to about 130, from about 10 to about 120, from about 10 to about 110, from about 10 to about 95, from about 10 to about 90, from about 20 to about 80, from about 30 to about 70, from about 30 to about 60, from about 30 to about 50, from about 30 to about 40, or about 32.

The nucleotide sequences disclosed herein may be used to detect Lactobacillus species, and/or to differentiate bacterial strains, including differentiating L. acidophilus NCFM® strains from other L. acidophilus strains. The detection and/or differentiation is based on the identification of novel CRISPR regions in L. acidophilus NCFM®, L. brevis, L. casei, and L. delbrueckii subspecies bulgaricus. As these CRISPR regions are strain-specific, any method assaying for the presence of these specific sequences is encompassed by the current invention. The present invention is applicable to medical testing, food testing, agricultural testing, and environmental testing.

Diagnostic assays to detect the presence of a nucleic acid molecule in a sample are disclosed. These methods comprise obtaining a sample, amplifying a region of DNA comprising at least one of SEQ ID NOS:1-7 and 37-48, or a variant thereof, to create amplified DNA, and detecting the amplified DNA. Detection of amplified DNA is specific for a Lactobacillus species. Different strains of a species of Lactobacillus, such as a L. acidophilus species, may have different sizes of amplified DNA. Therefore, this method may also be used as a tool for strain differentiation. The method may further comprise sequencing the amplified DNA and detecting the presence of a Lactobacillus species, such as L. acidophilus, L. brevis, L. casei, or L. delbrueckii, based on the sequencing results. Alternatively, the method may further comprise adding to the amplified DNA at least one restriction enzyme that recognizes one or more sites in the amplified DNA, incubating the restriction enzyme with the amplified DNA for a time sufficient to form restriction fragments, determining the number and size of the restriction fragments, and detecting the presence of a Lactobacillus species, such as L. acidophilus, L. brevis, L. casei, or L. delbrueckii, based on the number and size of the restriction fragments.

Methods for typing a Lactobacillus bacterial strain are provided. These methods comprise obtaining a sample, amplifying a region of DNA comprising at least one of the nucleotide sequences set forth in SEQ ID NOS:1-7 and 37-48, or a variant thereof, in the sample to create amplified DNA, and typing the bacterial strain based on the amplified DNA. This typing may be done by adding to the amplified DNA at least one restriction enzyme that recognizes one or more sites in the amplified DNA, incubating the restriction enzyme with the amplified DNA for a time sufficient to form restriction fragments, determining the number of the restriction fragments and their size, and typing the bacterial strain based on the number and size of the restriction fragments. Typing may also be done by sequencing the amplified DNA, and typing the bacterial strain based on the sequencing results. In one embodiment, the region of DNA to be amplified comprises SEQ ID NO:1. In another embodiment, the region of DNA comprises a nucleotide sequence having at least 75% sequence identity to at least one of SEQ ID NOS:1-7 and 37-48.

The amplified DNA may be obtained by providing a first primer that binds to a region of DNA flanking the CRISPR region, such as DNA upstream of the CRISPR region, and a second primer that binds to a region of DNA flanking the CRISPR region, such as DNA downstream of the CRISPR region; using the primers in a PCR reaction to create amplified DNA; separating the amplified DNA on a gel to produce a band showing the size of the amplified CRISPR DNA; and typing the bacterial strain based on the band size. The size of the amplified DNA is characteristic of the strain of Lactobacillus. In one embodiment, the first primer binds to a region of DNA upstream of the CRISPR region, such as that set forth in SEQ ID NO:49, and the second primer binds to a region of DNA downstream of the CRISPR region, such as that set forth in SEQ ID NO:50.

Alternatively, the amplified DNA may be obtained by providing a first primer that binds to a repetitive sequence in a CRISPR region; providing a second primer that binds to DNA flanking (i.e. upstream or downstream of) the CRISPR region; using the primers in a PCR reaction to create amplified DNA; separating the amplified DNA on a gel to produce a distinct band pattern showing the number and sizes of the amplified DNA; and typing the bacterial strain based on the pattern. The number and sizes of the bands are diagnostic of the strain of Lactobacillus. In one embodiment, the first primer binds to any of SEQ ID NOS:2-7 and 37-48, and the second primer binds to DNA flanking any of SEQ ID NOS:2-7 and 37-48.

This method wherein one primer binds to any of SEQ ID NOS:2-7 and 37-48 produces a number of bands of varying sizes, depending on the number and spacing of the repeats in relation to the anchored primer. For example, if the repeat region is present five times, the primer complementary to the repeat region will bind in five places and generate five bands that may be visualized as a fingerprint on an agarose or polyacrylamide gel. The PCR products may be amplified to different extents, and some of the resulting bands may therefore not be visualized as easily as others, if at all. The distinct band pattern shows the number and size of the amplified DNA, and may be used to characterize Lactobacillus strains, including L. acidophilus, L. brevis, L. casei, and L. delbrueckii strains.

The term “sample” is intended to include tissues, cells, and biological fluids present in or isolated from a subject, as well as cells from starter cultures (mother, seed, bulk/set, concentrated, dried, lyophilized, frozen), or food/dairy/feed products carrying such cultures, or derived from the use of such cultures. The sample may be a dietary supplement, bioprocessing fermentate, or a subject that has ingested a substance comprising the nucleotide sequence. That is, the detection method of the invention can be used to detect genomic DNA comprising a disclosed nucleotide sequence in a sample both in vitro and in vivo. In vitro techniques for detection of genomic DNA comprising the disclosed nucleotide sequences include, but are not limited to, Southern hybridizations. Results obtained with a sample from the food, supplement, culture, product, or subject may be compared to results obtained with a sample from a control culture, product, or subject. In one embodiment, the sample contains genomic DNA from a starter culture.

Amplification of the desired region of DNA may be achieved by any method known in the art, including polymerase chain reaction (PCR). By “amplification” is intended the production of additional copies of a nucleic acid sequence. This is generally carried out using PCR technologies well known in the art (Dieffenbach and Dveksler (1995) PCR Primer, a Laboratory Manual (Cold Spring Harbor Press, Plainview, N.Y.). By “polymerase chain reaction” or “PCR” is intended a method such as that disclosed in U.S. Pat. Nos. 4,683,195 and 4,683,202, herein incorporated by reference, which describe a method for increasing the concentration of a segment of a target sequence in a mixture of genomic DNA without cloning or purification. The length of the amplified segment of the desired target sequence is determined by the relative positions of two oligonucleotide primers with respect to each other, and therefore, this length is a controllable parameter. By virtue of the repeating aspect of the process, the method is referred to as “PCR”. Because the desired amplified segments of the target sequence become the predominant sequences (in terms of concentration) in the mixture, they are said to be “PCR amplified.”

In a PCR approach, oligonucleotide primers can be designed for use in PCR reactions to amplify all or part of the CRISPR locus. By “primer” is intended an oligonucleotide, whether occurring naturally as in a purified restriction digest or produced synthetically, which is capable of acting as a point of initiation of synthesis when placed under conditions in which synthesis of a primer extension product which is complementary to a nucleic acid strand is induced (i.e., in the presence of nucleotides and an inducing agent such as DNA polymerase and at a suitable temperature and pH). The primer is preferably single stranded for maximum efficiency in amplification, but may alternatively be double stranded. If double stranded, the primer is first treated to separate its strands before being used to prepare extension products. Preferably, the primer is an oligodeoxyribonucleotide. The primer must be sufficiently long to prime the synthesis of extension products in the presence of the inducing agent. The exact lengths of the primers will depend on many factors, including temperature, source of primer, and the use of the method. PCR primers are preferably at least about 10 nucleotides in length, and most preferably at least about 20 nucleotides in length.

Compositions of the invention include oligonucleotide primers that may be used to amplify these repetitive regions. Examples of PCR primers that may be used in the methods of the invention include primers that bind to a region of genomic DNA flanking the CRISPR region, such as those found in SEQ ID NOS:49 and 50, or a primer that binds to SEQ ID NO:36, or primers that bind within the CRISPR region, or a combination thereof. The forward and reverse primers are designed to amplify all or part of a CRISPR region. By “flanking” is intended a region 5′ (upstream) or 3′ (downstream) of the sequence. In some embodiments, at least one primer binds to a DNA sequence flanking the CRISPR region. In some embodiments, one primer binds to the first repetitive sequence (for example, SEQ ID NO:2) and one primer binds to a flanking DNA sequence (for example, SEQ ID NO:36), therefore amplifying the entire CRISPR region. In some embodiments, both primers bind to regions of DNA flanking the CRISPR region. Primers that are designed to bind to DNA flanking a CRISPR region would be species specific, as this flanking DNA would not be expected to share enough sequence identity between all Lactobacillus species.

The repetitive sequences in these CRISPR regions show nucleotide homology to each other (see FIG. 7). The L. acidophilus repetitive sequences are at least 86% identical to each other. The L. brevis repetitive sequences are at least 82% identical to each other. The L. delbrueckii ssp. bulgaricus repetitive sequences are at least 89% identical to each other. The L. acidophilus repetitive sequences are at least 57% identical to the L. brevis repetitive sequences. The L. acidophilus repetitive sequences are at least 71% identical to the L. casei repetitive sequences. The L. acidophilus repetitive sequences are at least 75% identical to the L. delbrueckii repetitive sequences. The L. brevis repetitive sequences are at least 64% identical to the L. casei repetitive sequences. The L. brevis repetitive sequences are at least 64% identical to the L. delbrueckii repetitive sequences. The L. casei repetitive sequences are at least 71% identical to the L. delbrueckii repetitive sequences.

When the DNA sequence flanking the CRISPR region is known, one of skill in the art would be able to design primers for amplifying the CRISPR region based on this known flanking sequence. When the DNA sequence flanking the CRISPR region is not yet known, one of skill in the art would be able to determine this flanking sequence using methods known in the art. The entire genome of L. acidophilus NCFM is provided in U.S. Provisional Application No. 60/622,712, and Altermann et al. (2005) Proc. Natl. Acad. Sci. U.S.A. 102:3906-3912, herein incorporated by reference in their entirety. The genome of L. plantarum is provided in Kleerebezem et al. (2003) Proc. Natl. Acad. Sci. U.S.A. 100:1990-1995. The entire genome of L. johnsonii is provided in Pridmore et al. (2004) Proc. Natl. Acad. Sci. U.S.A 101:2512-2517.

Methods for designing PCR primers and PCR cloning are generally known in the art and are disclosed in Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual (2d ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y.). See also Innis et al., eds. (1990) PCR Protocols: A Guide to Methods and Applications (Academic Press, New York); Innis and Gelfand, eds. (1995) PCR Strategies (Academic Press, New York); and Innis and Gelfand, eds. (1999) PCR Methods Manual (Academic Press, New York). Known methods of PCR include, but are not limited to, methods using paired primers, nested primers, single specific primers, degenerate primers, gene-specific primers, vector-specific primers, partially mismatched primers, and the like.

With PCR, it is possible to amplify a single copy of a specific target sequence to a level detectable by several different methodologies (e.g., hybridization with a labeled probe; incorporation of biotinylated primers followed by avidin-enzyme conjugate detection; incorporation of ³²P-labeled deoxynucleotide triphosphates, such as dCTP or dATP, into the amplified segment). In addition to genomic DNA, any oligonucleotide sequence can be amplified with the appropriate set of primer molecules. In particular, the amplified segments created by the PCR process itself are, themselves, efficient templates for subsequent PCR amplifications.

Amplification in PCR requires “PCR reagents” or “PCR materials,” which herein are defined as all reagents necessary to carry out amplification except the polymerase, primers, and template. PCR reagents normally include nucleic acid precursors (dCTP, dTTP, etc.), and buffer.

Once the DNA comprising the CRISPR locus or a portion thereof has been amplified, it may then be digested (cut) with a restriction enzyme. As used herein, the terms “restriction endonucleases” and “restriction enzymes” refer to bacterial enzymes, each of which cut double-stranded DNA at or near a specific nucleotide sequence. Restriction enzymes are well known in the art and may be readily obtained, for example, from variety of commercial sources (for example, New England Biolabs, Inc., Beverly, Mass.). Similarly, methods for using restriction enzymes are also generally well known and routine in the art. Preferred restriction enzymes are those that produce between 10 and 24 fragments of DNA when cutting the CRISPR locus (for example, SEQ ID NO:1). Examples of such enzymes include, but are not limited to, AluI, MseI, and Tsp5091. Fragments of DNA obtained using restriction enzymes may be detected, for example, as bands by gel electrophoresis. Restriction enzymes may be used to create Restriction Fragment Length Polymorphisms (RFLPs). RFLPs are, in essence, unique fingerprint snapshots of a piece of DNA, whether a whole chromosome (genome), or a part thereof, such as the region of the genome comprising the novel L. acidophilus CRISPR locus disclosed in the present invention.

RFLPs are generated by cutting (“restricting”) a DNA molecule with a restriction endonuclease. Many hundreds of such enzymes have been isolated, as naturally made by bacteria. In essence, bacteria use such enzymes as a defensive system, to recognize and then cleave (restrict) any foreign DNA molecules that might enter the bacterial cell (e.g., a viral infection). Each of the many hundreds of different restriction enzymes has been found to cut (i.e., “cleave” or “restrict”) DNA at a different sequence of the 4 basic nucleotides (A, T, G, C) that make up all DNA molecules, e.g., one enzyme might specifically and only recognize the sequence A-A-T-G-A-C, while another might specifically and only recognize the sequence G-T-A-C-T-A, etc. Depending on the unique enzyme involved, such recognition sequences may vary in length, from as few as 4 nucleotides to as many as 21 nucleotides. The larger the recognition sequence, the fewer restriction fragments will result, as the larger the recognition site, the lower the probability that it will repeatedly be found throughout the DNA.

Following the digestion, the resultant individual fragments are separated from one another based on their size. Any method suitable for separating DNA is encompassed by the methods of the present invention, including, but not limited to, gel electrophoresis, high performance liquid chromatography (HPLC), mass spectroscopy, and use of a microfluidic device. In one embodiment, the DNA fragments are separated by agarose gel electrophoresis. Gel electrophoresis separates different sized charged molecules by their rate of movement through a stationary gel under the influence of an electric current. These separated DNA fragments can easily be visualized, for example, by staining with ethidium bromide and by viewing the gel under UV illumination. The banding pattern reflects the sizes of the restriction digested DNA.

Alternatively to performing RFLP on the amplified CRISPR locus, the sequence of the amplified DNA may be obtained by any method known in the art, including automatic and manual sequencing methods. See, for example, Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual (2d ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y.; Roe et al. (1996) DNA Isolation and Sequencing (Essential Techniques Series, John Wiley & Sons).

Other methods that utilize the novel CRISPR repetitive regions of the invention to detect and/or type Lactobacillus strains are also encompassed by the invention. These methods include hybridization methods, either using a nucleic acid molecule of the invention as a probe, or a nucleic acid molecule capable of hybridizing to a disclosed nucleotide sequence of the present invention. See, for example, Sambrook et al. (1989) Molecular Cloning: Laboratory Manual (2d ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y.).

In hybridization techniques, the hybridization probe(s) may be genomic DNA fragments, PCR-amplified products, or other oligonucleotides, and may comprise all or part of a known nucleotide sequence disclosed herein. In addition, it may be labeled with a detectable group such as ³²P, or any other detectable marker, such as other radioisotopes, a fluorescent compound, an enzyme, or an enzyme co-factor. The term “labeled,” with regard to the probe, is intended to encompass direct labeling of the probe by coupling (i.e., physically linking) a detectable substance to the probe, as well as indirect labeling of the probe by reactivity with another reagent that is directly labeled. Examples of indirect labeling include end-labeling of a DNA probe with biotin such that it can be detected with fluorescently labeled streptavidin.

Probes for hybridization can be made by labeling synthetic oligonucleotides based on the known CRISPR region nucleotide sequences disclosed herein. In one embodiment the entire L. acidophilus CRISPR region nucleotide sequence (SEQ ID NO:1) is used as a probe to detect and/or differentiate an L. acidophilus strain. In another embodiment, the probe is a fragment of a nucleotide sequence disclosed herein, such as a probe consisting of a single repetitive sequence, as found in any of SEQ ID NOS:2-7 and 37-48. In yet another embodiment, the probe is a sequence found in a spacer region, for example in any of SEQ ID NOS:8-35. In another embodiment, the probe is a flanking region, such as that of SEQ ID NO:36. The hybridization probe typically comprises a region of nucleotide sequence that hybridizes under stringent conditions to at least about 10, preferably about 20, more preferably about 50, 75, 100, 125, 150, 175, 200, 250, 300, 350, or 400 consecutive nucleotides of a CRISPR region nucleotide sequence of the invention or a fragment or variant thereof. Preparation of probes for hybridization is generally known in the art and is disclosed in Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual (2d ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y.), herein incorporated by reference.

Substantially identical sequences will hybridize to each other under stringent conditions. By “stringent conditions” is intended conditions under which a probe will hybridize to its target sequence to a detectably greater degree than to other sequences (e.g., at least 2-fold over background). Stringent conditions are known in the art and can be found in Current Protocols in Molecular Biology (John Wiley & Sons, New York (1989)), 6.3.1-6.3.6.

When using probes, stringent conditions will be those in which the salt concentration is less than about 1.5 M Na ion, typically about 0.01 to 1.0 M Na ion concentration (or other salts) at pH 7.0 to 8.3 and the temperature is at least about 30° C. for short probes (e.g., 10 to 50 nucleotides) and at least about 60° C. for long probes (e.g., greater than 50 nucleotides).

The post-hybridization washes are instrumental in controlling specificity. The two critical factors are ionic strength and temperature of the final wash solution. For the detection of sequences that hybridize to a full-length or approximately full-length target sequence, the temperature under stringent conditions is selected to be about 5° C. lower than the thermal melting point (T_(m)) for the specific sequence at a defined ionic strength and pH. However, stringent conditions would encompass temperatures in the range of 1° C. to 20° C. lower than the T_(m), depending on the desired degree of stringency as otherwise qualified herein. For DNA-DNA hybrids, the T_(m) can be determined using the equation of Meinkoth and Wahl (1984) Anal. Biochem. 138:267-284: T_(m)=81.5° C.+16.6 (log M)+0.41 (% GC)−0.61 (% form)−500/L; where M is the molarity of monovalent cations, % GC is the percentage of guanosine and cytosine nucleotides in the DNA, % form is the percentage of formamide in the hybridization solution, and L is the length of the hybrid in base pairs. The T_(m) is the temperature (under defined ionic strength and pH) at which 50% of a complementary target sequence hybridizes to a perfectly matched probe.

The ability to detect sequences with varying degrees of homology can be obtained by varying the stringency of the hybridization and/or washing conditions. To target sequences that are 100% identical (homologous probing), stringency conditions must be obtained that do not allow mismatching. By allowing mismatching of nucleotide residues to occur, sequences with a lower degree of similarity can be detected (heterologous probing). For every 1% of mismatching, the T_(m) is reduced about 1° C.; therefore, hybridization and/or wash conditions can be manipulated to allow hybridization of sequences of a target percentage identity. For example, if sequences with >90% sequence identity are preferred, the T_(m) can be decreased by 10° C.

Exemplary low stringency conditions include hybridization with a buffer solution of 30-35% formamide, 1 M NaCl, 1% SDS (sodium dodecyl sulfate) at 37° C., and a wash in 1× to 2×SSC (20×SSC=3.0 M NaCl/0.3 M trisodium citrate) at 50 to 55° C. Exemplary moderate stringency conditions include hybridization in 40 to 45% formamide, 1.0 M NaCl, 1% SDS at 37° C., and a wash in 0.5× to 1×SSC at 55 to 60° C. Exemplary high stringency conditions include hybridization in 50% formamide, 1 M NaCl, 1% SDS at 37° C., and a wash in 0.1×SSC at 60 to 65° C. Optionally, wash buffers may comprise about 0.1% to about 1% SDS. Duration of hybridization is generally less than about 24 hours, usually about 4 to about 12 hours. An extensive guide to the hybridization of nucleic acids is found in Tijssen (1993) Laboratory Techniques in Biochemistry and Molecular Biology—Hybridization with Nucleic Acid Probes, Part I, Chapter 2 (Elsevier, New York); and Ausubel et al., eds. (1995) Current Protocols in Molecular Biology, Chapter 2 (Greene Publishing and Wiley-Interscience, New York). See Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual (2d ed., Cold Spring Harbor Laboratory Press, Plainview, N.Y.).

Methods that encompass hybridization techniques to detect or differentiate bacterial strains are also encompassed. These include, but are not limited to, Southern blotting (see, for example, Van Embden et al. (1993) J. Clin. Microbiol. 31:406-409), shift mobility assays (see, for example, U.S. Published Application No. 20030219778), sequencing assays using oligonucleotide arrays (see, for example, Pease et al. (1994) Proc. Natl. Acad. Sci. USA 91:5022-5026), spoligotyping (see, for example, Kamerbeek et al. (1997) J. Clin. Microbiol. 35:907-914), Flourescent In Situ Hybridization (FISH) (see, for example, Amann et al. (1990) J. Bacteria 172:762-770) and heteroduplex tracking assays or heteroduplex mobility analysis (see, for example, White et al. (2000) J. Clin. Micro. 38:477-482).

The invention also encompasses kits for detecting the presence of the nucleic acids of the present invention in a sample. Such kits can be used for typing or detection of Lactobacillus strains present in, for example, a food product or starter culture, or in a subject that has consumed a probiotic material. For example, the kit may comprise PCR primers for amplification of a CRISPR locus, as well as a polymerase and other PCR materials for use in DNA amplification. The kit may also contain one or more restriction enzymes for use in RFLP analysis. The kit may contain a labeled compound or agent capable of detecting a disclosed nucleic acid sequence in a sample and means for determining the amount of a the disclosed nucleic acid sequence in the sample (e.g., an oligonucleotide probe that binds to a nucleic acid sequence of the invention, e.g., any of SEQ ID NOS:1-50).

For oligonucleotide-based kits, the kit may comprise, for example: (1) an oligonucleotide, e.g., a detectably labeled oligonucleotide, that hybridizes to a disclosed nucleic acid sequence, or (2) a pair of primers useful for amplifying a disclosed nucleic acid molecule.

The kit may also comprise, e.g., a buffering agent, a preservative, or a protein-stabilizing agent. The kit may also comprise components necessary for detecting the detectable agent (e.g., an enzyme or a substrate). The kit may also contain a control sample or a series of control samples (both positive and negative) that can be assayed and compared to the test sample contained. Each component of the kit is usually enclosed within an individual container, and all of the various containers are within a single package along with instructions for use.

In one embodiment, the kit comprises multiple probes in an array format, such as those described, for example, in U.S. Pat. Nos. 5,412,087 and 5,545,531, and International Publication No. WO 95/00530, herein incorporated by reference. Probes for use in the array may be synthesized either directly onto the surface of the array, as disclosed in International Publication No. WO 95/00530, or prior to immobilization onto the array surface (Gait, ed. (1984) Oligonucleotide Synthesis a Practical Approach (IRL Press, Oxford, England). The probes may be immobilized onto the surface using techniques well known to one of skill in the art, such as those described in U.S. Pat. No. 5,412,087. Probes may be a nucleic acid or peptide sequence, preferably purified.

The arrays may be used to screen organisms, samples, or products to differentiate between Lactobacillus strains, or to verify the presence of a Lactobacillus species, such as L. acidophilus NCFM®. Binding to a capture probe is detected, for example, by signal generated from a label attached to the nucleic acid molecule comprising the disclosed nucleic acid sequence. The method can include contacting the molecule comprising the disclosed nucleic acid with a first array having a plurality of capture probes and a second array having a different plurality of capture probes. The results of each hybridization can be compared to analyze differences in the content between a first and second sample. The first plurality of capture probes can be from a control sample, e.g., a sample known to contain L. acidophilus NCFM®, or control subject, e.g., a food, including an animal feed or animal feed supplement, a dietary supplement, a starter culture sample, or a biological fluid. The second plurality of capture probes can be from an experimental sample, e.g., a subject that has consumed a probiotic material, a starter culture sample, a food, or a biological fluid.

These assays may be especially useful in microbial selection and quality control procedures where the detection of unwanted materials is essential. The detection of particular nucleotide sequences may also be useful in determining the genetic composition of food, fermentation products, or industrial microbes, or microbes present in the digestive system of animals or humans that have consumed probiotics.

Fragments and Variants

The invention includes isolated nucleic acid molecules comprising the nucleotide sequence of a CRISPR locus from L. acidophilus, L. brevis, L. casei, L. delbrueckii, or variants and fragments thereof. By “fragment” of a nucleic acid molecule is intended a portion of the nucleotide sequence. Fragments of nucleic acid molecules can be used as hybridization probes to detect and/or differentiate CRISPR regions from various bacteria, including Lactobacillus species, or can be used as primers in PCR amplification of CRISPR regions. Fragments of nucleic acids can also be bound to a physical substrate to comprise what may be considered a macro- or microarray (for example, U.S. Pat. Nos. 5,837,832 and 5,861,242). Such arrays of nucleic acids may be used to identify nucleic acid molecules with sufficient identity to the target sequences. By “nucleic acid molecule” is intended DNA molecules (e.g., cDNA or genomic DNA) and RNA molecules (e.g., mRNA) and analogs of the DNA or RNA generated using nucleotide analogs. The nucleic acid molecule can be single-stranded or double-stranded, but preferably is double-stranded DNA. A nucleotide fragment may be used as a hybridization probe or PCR primer as described above. Fragments of CRISPR region nucleic acid molecules comprise at least about 15, 20, 50, 75, 100, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, 1000, 1100, 1200, 1300, 1400, 1500, 1600, 1700, 1800, 1900 nucleotides or up to the total number of nucleotides present in a full-length CRISPR region nucleotide sequence as disclosed herein (for example, 1953 for SEQ ID NO:1).

Variants of the nucleotide sequences are encompassed in the present invention. By “variant” is intended a sufficiently identical sequence. Accordingly, the invention encompasses isolated nucleic acid molecules that are sufficiently identical to any of the nucleotide sequences of SEQ ID NOS:1-50, or nucleic acid molecules that hybridize to any of the nucleotide sequences of SEQ ID NOS:1-50, or a complement thereof, under stringent conditions.

In general, nucleotide sequences that have at least about 45%, 55%, or 65% identity, preferably at least about 70% or 75% identity, more preferably at least about 78%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, or 90%, most preferably at least about 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% sequence identity to any of the nucleotide sequences of SEQ ID NOS:1-50, are defined herein as sufficiently identical.

Naturally occurring variants may exist within a population (e.g., the L. acidophilus population). Such variants can be identified by using well-known molecular biology techniques, such as PCR, and hybridization as described above. Synthetically derived nucleotide sequences, for example, sequences generated by site-directed mutagenesis or PCR-mediated mutagenesis, that still allow strain differentiation or detection, are also included as variants. One or more nucleotide substitutions, additions, or deletions can be introduced into a nucleotide sequence disclosed herein, such that the substitutions, additions, or deletions do not affect the ability to differentiate strains based on any of the methods disclosed herein or known in the art, including, but not limited to RFLP, sequencing, and hybridization. Examples of variants of a CRISPR repeat region can be found in SEQ ID NOS:2-7 and 37-48.

Sequence Identity

The nucleotide sequences encompassed by the present invention have a certain sequence identity. By “sequence identity” is intended the nucleotide residues that are the same when aligning two sequences for maximum correspondence over a specified comparison window. By “comparison window” is intended a contiguous segment of the two nucleotide sequences for optimal alignment, wherein the second sequence may contain additions or deletions (i.e., gaps) as compared to the first sequence. Generally, for nucleic acid alignments, the comparison window is at least 20 contiguous nucleotides in length, and optionally can be 30, 40, 50, 100, or longer. Those of skill in the art understand that to avoid a high similarity due to inclusion of gaps, a gap penalty is typically introduced and is subtracted from the number of matches.

To determine the percent identity of two nucleotide sequences, an alignment is performed. Percent identity of the two sequences is a function of the number of identical residues shared by the two sequences in the comparison window (i.e., percent identity=number of identical residues/total number of residues×100). In one embodiment, the sequences are the same length. Methods similar to those mentioned below can be used to determine the percent identity between two sequences. The methods can be used with or without allowing gaps.

Mathematical algorithms can be used to determine the percent identity of two sequences. Non-limiting examples of mathematical algorithms are the algorithm of Karlin and Altschul (1990) Proc. Natl. Acad. Sci. USA 87:2264, modified as in Karlin and Altschul (1993) Proc. Natl. Acad. Sci. USA 90:5873-5877; the algorithm of Myers and Miller (1988) CABIOS 4:11-17; the local homology algorithm of Smith et al. (1981) Adv. Appl. Math. 2:482; the global alignment algorithm of Needleman and Wunsch (1970) J. Mol. Biol. 48:443-453; and the search-for-local alignment-method of Pearson and Lipman (1988) Proc. Natl. Acad. Sci. USA 85:2444-2448.

Various computer implementations based on these mathematical algorithms have been designed to enable the determination of sequence identity. The BLAST programs of Altschul et al. (1990) J. Mol. Biol. 215:403 are based on the algorithm of Karlin and Altschul (1990) supra. Searches to obtain nucleotide sequences that are homologous to nucleotide sequences of the present invention can be performed with the BLASTN program, score=100, wordlength=12. Gapped alignments may be obtained by using Gapped BLAST (in BLAST 2.0) as described in Altschul et al. (1997) Nucleic Acids Res. 25:3389. To detect distant relationships between molecules, PSI-BLAST can be used. See, Altschul et al. (1997) supra. For all of the BLAST programs, the default parameters of the respective programs can be used. See, www.ncbi.nlm.nih.gov. Alignment may also be performed manually by inspection.

Another program that can be used to determine percent sequence identity is the ALIGN program (version 2.0), which uses the mathematical algorithm of Myers and Miller (1988) supra. In addition to the ALIGN and BLAST programs, the BESTFIT, GAP, FASTA and TFASTA programs are part of the GCG Wisconsin Genetics Software Package, Version 10 (available from Accelrys Inc., 9685 Scranton Rd., San Diego, Calif., USA), and can be used for performing sequence alignments. The preferred program is GAP version 10, which used the algorithm of Needleman and Wunsch (1970) supra. Unless otherwise stated the sequence identity values provided herein refer to those values obtained by using GAP Version 10 with the following parameters: % identity using GAP Weight of 50 and Length Weight of 3 and the nwsgapdna.cmp scoring matrix. Other equivalent programs may also be used. By “equivalent program” is intended any sequence comparison program that, for any two sequences in question, generates an alignment having identical nucleotide residue matches and an identical percent sequence identity when compared to the corresponding alignment generated by GAP Version 10.

The following examples are offered by way of illustration and not by way of limitation.

EXPERIMENTAL Example 1 DNA Analysis

The genomic DNA sequence from Lactobacillus acidophilus NCFM® was analyzed for repetitive DNA by a “repeat and match analysis” using Applied Maths' Kodon software package. One intergenic region between DNA polymerase I (polA) (ORF 1550) and a putative phosphoribosylamine-glycine ligase (purD) (ORF 1551) was identified as having features characteristic of a CRISPR locus. This region is approximately 2.4 kb long and contains 32 nearly perfect repeats of 29 base pairs separated by 32 base pair spacers (see FIGS. 1 and 2).

A number of features of the CRISPR region can be seen in FIG. 2. The 29 base pair repeats are highlighted. The first nucleotide of the repeat is either an A or a G. The last nucleotide of the repeat changes from a T to a C at repeat number 21. An imperfect inverted repeat is indicated by an underline on the last repeat. The first repeat contains two A→T base substitutions. The 26^(th) repeat contains one C→T base substitution. Two sequences are repeated in the spacer region; one is repeated twice (bolded and outlined) and one is repeated three times (bolded and caps). The 16^(th) spacer region is one base longer than the others.

Example 2 PCR of Intergenic Region

Primers were designed to amplify the entire intergenic region between polA and purD (expected product size=2582 base pairs). The primers were as follows:

(SEQ ID NO: 49) 1550_F- 5′ GCA TTA GTG TGC AAC CCA TCT GG 3′ (SEQ ID NO: 50) 1551_R- 5′ GAT CTG CTG GAT TGC TTC TAC CG 3′

A PCR reaction mix was set up for each reaction (25.0 μl of AccuPrime SuperMix II (2× conc.); 1.0 μl of each primer (20 μM); 1 μl of template (300 ng/μl); H₂O to 50.0 μl). The reaction conditions were as follows: 1 cycle at 95° C. for 5 minutes; 40 cycles with a first step at 95° C. for 30 seconds, a second step at 54° C. for 30 seconds, and a third step at 68° C. for 3 minutes; 1 cycle at 68° C. for 7 minutes.

This PCR was performed on sixteen L. acidophilus strains. All L. acidophilus strains that had previously been shown to be identical to L. acidophilus NCFM® by other means (i.e., PFGE, Microarrays, 16S sequencing, etc.) generated the same size PCR amplicon. Three strains that had previously been shown to be different from NCFM® (ATCC 4356, ATCC 4357, and Strain B) exhibited different sized amplicons. Strains of Lactobacillus helveticus, Lactobacillus gasseri, and Lactobacillus plantarum that were tested did not generate a PCR product.

Four strains were found that did not generate a PCR product: L. acidophilus ATCC 521, L. acidophilus strain F, L. acidophilus strain G, and L. acidophilus strain H. These strains were sent to MIDI Labs for identification and were identified as follows:

L. acidophilus ATCC 521 L. helveticus L. acidophilus strain F Pediococcus parvulus L. acidophilus strain G L. gasseri L acidophilus strain H L. plantarum

The PCR results for 6 strains are shown in FIG. 3A. The different sized bands indicated that there were significant differences in the CRISPR region of some strains.

Example 3 PCR Amplification Method is Specific for Lactobacillus acidophilus Detection

PCR was performed on 23 bacterial samples as described in Example 2. PCR amplification of all L. acidophilus strains tested resulted in a PCR amplicon, whereas all other species tested did not (see FIG. 4). The species of all tested strains were confirmed using 16S sequencing. Therefore, this method is specific for L. acidophilus.

Example 4 Restriction Digestion of Intergenic Region

In order to generate more discriminatory patterns for each strain, the CRISPR PCR products were subjected to restriction digestion with three enzymes that generated between 10 and 24 bands: AluI—10 bands; MseI—19 bands; Tsp509I—24 bands.

AluI: Six CRISPR PCR products were digested with AluI and separated on a 2% agarose gel (FIG. 3B). Three strains exhibited a difference in banding pattern, ATCC 4356, ATCC 4357, and strain B. These results are in agreement with the results of other tests (Microarray, Transposase-PCR, PFGE) that indicate these three strains are unique (data not shown).

MseI: Six CRISPR PCR products were digested with MseI and separated on a 3% agarose gel (FIG. 3C).

Tsp509I: Six CRISPR PCR products were digested with Tsp5091 and separated on a 3% agarose gel (FIG. 3D).

Example 5 PCR Amplification Followed by Enzymatic Digestion can Differentiate L. acidophilus Strains

Fourteen L. acidophilus strains were subjected to both CRISPR locus amplification and restriction enzyme digestion as described in Examples 2 and 4. Seven distinct band patterns were generated, indicating that this method can differentiate between strains (see FIG. 5).

Example 6 PCR/Digestion Products Match PFGE Results

PFGE was performed on the fourteen L. acidophilus strains discussed in Example 5. The PFGE results confirmed those obtained by using the PCR/Digestion Method as described in Examples 2-5 (see FIG. 6). NCFM® and Lac-1 strains showed identical PFGE and PCR/Digestion results, but differed from Lac-3 and ATCC4356.

Example 7 Identification of CRISPR Regions in Other Lactobacillus Species

Other Lactobacillus species were analyzed for CRISPR sequences as described in Example 1. CRISPR sequences were found in L. brevis, L. casei and L. delbrueckii ssp. bulgaricus. The repeat sequences are shown in FIG. 7, with variant nucleotides shown below the main sequences. Within the regions analyzed, 32 repeats were present in L. acidophilus, 12 repeats were present in L. brevis, 21 repeats were present in L. casei, and 17 repeats were present in L. delbrueckii ssp. bulgaricus.

Example 8 Strain Typing of Lactabacillus Species

Primers are designed to amplify the entire CRISPR region of L. delbrueckii ssp. bulgaricus. A PCR reaction mixture is set up and PCR is performed on ten L. delbrueckii ssp. bulgaricus strains, as described in Example 2. The PCR products are subjected to restriction digestion with AluI, MseI, and Tsp509I as described in Example 4. The DNA is separated by gel electrophoresis and the band patterns are analyzed. Detection of different band patterns indicates the presence of different strains of L. delbrueckii ssp. bulgaricus.

CONCLUSIONS

The identification of a unique CRISPR region in NCFM® is a promising discovery for the development of detection and differentiation methods. Of 20 strains designated as L. acidophilus tested, 16 generated a CRISPR-PCR fragment with the designed primers. The four strains for which no fragment was amplified were confirmed by MIDI Labs as being misidentified—strengthening the position of this CRISPR locus as being L. acidophilus specific. The remaining 16 strains were subjected to restriction analysis of the CRISPR-PCR fragment revealing 12 strains with identical restriction patterns and 3 strains with unique patterns. These results are supported by data that has been generated independently by comparative genome microarray analysis, transposase-PCR analysis, and PFGE.

In summary, a relatively quick and easy CRISPR-PCR/restriction analysis generated unique fragmentation patterns for the truly different L. acidophilus strains tested. The method can also be applied in other Lactobacillus species, including L. brevis, L. casei, and L. delbrueckii.

All publications and patent applications mentioned in the specification are indicative of the level of skill of those skilled in the art to which this invention pertains. All publications and patent applications are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference.

Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it will be obvious that certain changes and modifications may be practiced within the scope of the appended claims. 

1.-17. (canceled)
 18. A method for detecting the presence of a Lactobacillus species in a sample, comprising: a) obtaining a sample; b) amplifying a region of DNA comprising at least one of SEQ ID NOS: 1-48, or a variant thereof, to create amplified DNA; and, c) detecting said amplified DNA. 19.-20. (canceled) 